A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764243



Internal ID20540103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139572186..139572186hg38UCSC Ensembl
chr4:140493340..140493340hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764243
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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